Electronic device fabrication on non-conductive polymer substrate

ABSTRACT

A process for fabricating an electronic device on a non-conductive polymer substrate, particularly from the family of polyaniline, comprises applying a covalent doping agent, such as an R +   donor compound, where R is an organic group, e.g., methyl iodide, to a preselected portion of a base-type non-conductive polymer substrate containing carbon-nitrogen linkages, and converting such preselected portion of the polymer substrate to an electrically conductive polymer portion, by covalent linkage of the R groups of such donor compound, to nitrogen atoms of the non-conductive polymer substrate. Electronic devices, such as resistors, capacitors, inductors, printed circuits and the like, can be provided by the invention process, in the form of light-weight polymers containing no metal, and which are stable and wherein the conductive portions are non-diffusing.

BACKGROUND OF THE INVENTION

The present invention relates to the production of electronic devicesand is particularly concerned with a process for the fabrication ofelectronic devices employing a non-conductive polymer substrate,portions of which can be selectively rendered conductive by suitablechemical treatment.

The free-base form of polyaniline is electrically non-conductive.Protonic acid doping of polyaniline by reaction of polyaniline with aprotonic acid HX where X is, for example, Cl, to produce electricallyconductive polyaniline is known, for example, as disclosed in A. G.MacDiarmid, et al, Mol. Cryst. Liq. Cryst., 121, 173 (1985). Conductivepolyaniline of this type has been employed in batteries, as disclosed inFrench Pat. No. 1,519,729.

However, if a film or bulk polymer of a material, such as polyaniline,is subjected to treatment in preselected regions, as by normal protonicacid treatment, to form doped conductive regions, for example, to form aconductive strip, such conductive regions or strip remains conductivelystable only for a very short time, after which such conductive regionsdiffuse, causing the entire piece to have constant conductivity.

Further, base-type conductive polymers, as represented by the protonicacid-doped polyaniline class of conductive polymers, are unstable anddegrade when exposed to water. Stability on contact with water isextremely rare in prior art conducting polymers, such as produced bytreatment of polyaniline with protonic acids.

An object of the present invention is to enable the construction ofpolymeric electronic devices without the use of metals.

Another object of the invention is to provide a process for producingelectronic devices on a non-conductive polymer substrate which can beselectively converted by suitable treatment to provide conductiveportions which do not tend to diffuse.

Still another object is the provision of novel procedure for theproduction of electronic devices, as noted above, wherein theconductivity of the conducting portions of such devices does not degradeif the components of the device are exposed to water.

SUMMARY OF THE INVENTION

The above objects are achieved, according to the invention, by thecarbocation doping of preselected portions of a base-type non-conductivepolymeric substrate, particularly from the polyaniline family, to formconducting portions on the non-conductive substrate. This can beaccomplished, e.g., according to one embodiment, by applying a mask tothe non-conductive polymer substrate, leaving certain preselected areasor regions of the polymer substrate not covered by the mask exposed, andtreating the exposed areas of the polymer substrate, as by spraying,with an organic material of a type which reacts with the exposed polymerregions to render them conductive, by covalent linkage of the organicgroup to the nitrogen atoms of the polymer.

The base-type non-conductive polymer forming the substrate is of thetype which contains carbon-nitrogen linkages, as in polyaniline. Thematerial which is applied, as by spraying, immersion or brushing, to thepreselected exposed areas of the polymer substrate is an R+ donorcompound, where R is an organic cation group, such R group being capableof covalently binding to the nitrogens of the polymer, and forming anelectrically conductive polymer in which the R groups are covalentlylinked to the nitrogen atoms of the polymer, in the preselected orexposed portions of the substrate.

More particularly, in one embodiment, the preselected or exposedportions of the non-conductive polymer substrate containingcarbon-nitrogen linkages, particularly as represented by the free-basepolyaniline, can be treated and reacted with an R⁺ donor compound, suchas R⁺ X⁻ or R₃ O⁺ X⁻, where R⁺ is a strong donor, i.e., an organiccation, such as an alkyl group, e.g., CH₃ ⁺, and X⁻ is a stable anion,such as I⁻, e.g., as provided by CH₃ I, to form a polymer salt in whicha covalent bond is formed between a nitrogen and the orqanic R qroup.

The reaction of base-type non-conductive polymers, such as polyaniline,with a compound or agent of the above type to produce base-typeconducting polymers, is disclosed in my co-pending application, SerialNo. 920,474 filed Oct. 20, 1986, issued Jan. 17, 1989 as U.S. Pat. No.4,798,685 titled "Production of Base-Type Conducting Polymers", andassigned to the same assignee as the present application.

In another embodiment, such preselected portions of the non-conductivepolymer substrate containing carbonnitrogen linkages can be treated withan R⁺ donor compound, such as R₂ SO₄, R'SO₂ Cl, or R₃ "SiCl, where R⁺,R'SO₂ ⁺ or R₃ "Si⁺ is a strong donor or organic cation, and RSO₄ or theCl⁻ is a stable anion, to form a polymer salt in which a covalent bondis formed between the nitrogen of the polymer and such donor cation.

The reaction of base-type non-conductive polymers, such as polyaniline,with a compound, such as R₂ SO₄, R'SO₂ Cl, or R₃ "SiCl, to producebase-type conducting polymers, is disclosed in the co-pendingapplication, Ser. No. 013,305, filed Feb. 11, 1987, by Stuart I.Yaniger, et al, titled "Preparation of Base-Type Conductive Polymers",and assigned to the same assignee as the present application.

The resulting polymer substrate, following treatment with one of theabove compounds, has electrically conductive portions in pre-selectedareas surrounded by the non-conductive polymer substrate. In the exposedconductive, e.g., non-masked, areas wherein there is a covalent linkagebetween the above-noted donor cation groups and nitrogens in thepolymer, this results in pinning the conductive region, so that theregion to which the treating agent has been applied, e.g., in the formof a strip, remains conductive, with substantially no diffusion takingplace to other regions of the substrate. In addition, the preselectedconductive regions on the polymer substrate do not lose conductivity oncontact with water.

Utilizing the above concept, various electronic components which do notcontain metal can be fabricated according to the invention, which arestable, and have the advantages of light weight and flexibility,provided by the use of polymers, as substrate, and which can befabricated at relatively low cost. Electronic devices which can befabricated by the invention process include resistors, capacitors,inductors, printed circuits, electronic devices with components havingconductivity gradients, etc.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be more clearly understood by reference to thedetailed description of the invention, set forth hereinafter, taken inconjunction with the accompanying drawings wherein:

FIG. 1 illustrates the steps of the procedure according to theinvention, for fabricating a resistor;

FIG. 2 illustrates the steps of the invention process for producing acapacitor;

FIG. 3 is an enlarged cross-section of the capacitor produced by theprocess of FIG. 2, taken on line 3--3 of FIG. 2(c);

FIG. 4 illustrates the steps of the invention procedure for producing anelectronic component having conductivity gradients;

FIG. 5 illustrates the procedure for producing an inductor by theinvention procedure; and

FIG. 6 illustrates production of an electronic device having aconductive loop formed on a non-conductive polymeric substrate.

DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS

According to the invention, covalent doping of base-type non-conductivepolymers, e.g., polyaniline free-base substrates, in preselectedregions, yields non-diffusing conductive regions surrounded byinsulating polymer substrate. Thus, a passive electronic component canbe fabricated by exposure of preselected regions of the substrate basepolymer to chemical reactants, such as the above-noted R⁺ donorcompound, which cause the above-noted chemical reaction.

Referring to FIG. 1 of the drawing, illustrating a mode of procedure forproducing a resistor according to the invention, numeral 10 illustratesa base-type non-conductive polymer substrate to which a conductiveregion is to be applied. A preferred form of non-conductive base-typepolymer employed as substrate are those of the polyaniline family,including polyaniline and derivatives thereof containing naphthyl orbiphenyl groups or other aromatic groups, in place of the phenyl groupsof polyaniline. Such polymers can include alkyl and aryl substitutedpolyaniline and its alkyl and aryl substituted naphthyl and biphenylderivatives, e.g., 2-methyl biphenyl, butyl naphthalene, 2-methylaniline derivatives, beta phenyl naphthalene and beta tolyl naphthalene.Such polymeric substrates also can include other base-type polymerscontaining carbon atoms linked to nitrogen, such as cyanogen polymer ofthe type: ##STR1##

Another type of polymer substrate can include mixtures and blends of theabove non-conductive homopolymers and copolymers of the above polymersand other polymers, such as a blend of polyaniline andpolymethylmethacrylate, and polymer alloys, such aspolybenzinidazole-polyimide alloys, containing carbon-nitrogen groups.

Thus, the term "non-conductive polymer substrate" as employed herein isintended to denote any of the above homopolymer or copolymer materials.

The invention will be described hereinafter, however mostly in terms ofthe use of the preferred non-conductive free-base polyaniline asnon-conductive polymeric substrate. In the case of polyanilinefree-base, this is a high polymer having a molecular weight of the orderof 50,000 to 80,000. Lower molecular weight polyaniline, such asemeraldine, can be employed, which is an oligomer of polyanilinecontaining eight (8) subunits and having a molecular weight of about 800to 900.

There is applied to the surface of the non-conductive polymer substrate10 a mask 12 having a cut-out strip 14 therein. For this purpose, anyconventional maskant which is inert to the reactant or treating agentcan be employed. The maskant composition should also be inert withrespect to the base polymer of the substrate. For this purpose, metalmasks, such as stainless steel, can be employed. Other metals which canbe employed as maskant include platinum, gold, nickel, and the like. Themetal mask can be suitably adhered to the polymer substrate as bypressure contact, adhesive, and the like, but can be readily removedfollowing chemical treatment. Alternatively, organic maskants containingas an essential ingredient thereof an organic polymer, such as achloroprene polymer resin, or a styrene butadiene or a styrene ethylenebutylene co-polymer, can be employed.

The masked polymeric substrate 12, as seen in FIG. 1(b), is treated, asby spraying, to contact the exposed surface of the polymer substratewithin the cut-out area 14 of the mask, with the treating agent. Thetreating agent with which the exposed area 16 of the polymer substrateis contacted is an R⁺ donor compound, such as RX, R₃ OX, R₂ SO₄, R'SO₂Cl, or R₃ "SiCl, where R, R'SO₂ or R₃ "Si is a group which readily formsa covalent bond with nitrogen, and wherein R, R' and R" each can bealkyl, e.g., methyl, ethyl and the like, and aryl, e.g., p-toluenesulfonyl (tosyl), benzyl, tolyl, xylyl, and other aromatic moieties, andX is an anion such as halogen, e.g., Cl⁻, I⁻ or Br⁻ ; PF₆ ⁻, SbCl₆ ⁻,and substituted and unsubstituted benzene sulfonate, and the like. Theabove reaction forms a conductive polymer salt.

Thus, the reactant which forms a covalent chemical bond with thenitrogen of the polyaniline free-base or equivalent polymer noted above,can be, for examole, one of the above R⁺ donor compounds, such as analkyl halide, wherein the alkyl group can contain from 1 to 20 carbonatoms, such as methyl iodide, or dimethylsulfate, (CH₃ CH₂)₃ O⁺ SbCl₆ ⁻,(CH₃)₂ CHI, p--CH₃ --C₆ H₄ SO₂ Cl, (CH₃)₃ O⁺ PF₆, (CH₃)₃ OSO₃ C₆ H₄ CH₃and (CH₃)₃ SiCl. Also, multifunctional reagents, e.g., ClSO₂ --C₆ H₄--C₅ H₄ --SO₂ Cl can be employed. However, R, R' or R" also can be anoligomeric or group, e.g., containing from about 20 to about 100,000carbon atoms, e.g., polyvinyl iodide.

The reaction for converting the base-type non-conductive polymer portionin the exposed area 16 of the substrate to a conductive polymer can berepresented as follows, where RX or R₃ OX is the R+ donor compound:##STR2## where A is a carbon-containing group, such as aryl,particularly the benzene ring, and including naphthyl and biphenyl, andsubstituted benzene, naphthyl or bipheyl groups, such as the alkyl andaryl derivatives described above; R and X are as defined above, and y isan integer ranging from about 1 to about 1,000, e.g., about 10 to about100. When y is in the lower end of the above range, e.g., when y is 1 or2, the materials are known as oligomers and are intended to be includedwithin the term "polymer" employed herein.

Where the preferred non-conductive polymer employed as the basesubstrate is polyaniline free-base (PFB), the general reaction schemefor producing conductive polymer portions when employing the reactant RXor R₃ OX is represented below: ##STR3## where R, X and y have the valuesnoted above.

In the above representative reactions, it will be understood that the R⁺donor reactant can alternatively be R₂ SO₄, R'SO₂ Cl or R₃ "SiQ, where Qis a halogen, such as Cl or Br. If he reaction is carred out using R₂SO₄, R⁺ is the organic cation which is covalently linked to the N atomsof the polymer and X is the stable RSO₄ ⁻ anion. When R'SO₂ Cl is thereactant, the organic cation is the R'SO₂ ⁺ group, which is covalentlylinked to the N atoms of the polymer through the S atom of such grpup,and X is the stable Cl⁻ anion. When R₃ "SiCl is the reactant, theorganic cation is the R₃ "Si⁺ group, which is covalently linked to the Natoms of the polymer through the Si atom of such group, and X is thestable Cl⁻ anion. When R₃ "SiCl is the reactant, the organic cation isthe R₃ "Si⁺ group, which is covalently linked to the N atoms of thepolymer through the Si atom of such group, and X is the stable Cl⁻anion.

The reaction can be carried out as a heterogenuous reaction wherein thereactant, e.g., RX, per se, is reacted with the exposed polymersubstrate portion, such as polyaniline free-base, or the reactant can bedissolved in a suitable solvent which does not irreversibly react withthe R⁺ donor, such as, e.g., methylene chloride, tetrahydrofuran (THF),acetonitrile, pyridine, dimethylsulfoxide (DMSO) and dimethylformamide(DMF). However, when employing an R₃ OX donor compound, such as (CH₃)₃OX and acetonitrile as solvent, the (CH₃)₃ O⁺ group can react with theCH₃ C═N solvent to form CH₃ C═N⁺ --CH₃ which can also function as amethyl cation donor.

The rate of reaction can range widely, depending on the particular R⁺donor or reactant employed, and the period of exposure of the exposedpolymer substrate portion 16 to the reactant. If the reaction betweenthe exposed polymer, e.g., polyaniline, substrate portion and the R⁺donor compound is carried to completion, the cation or R group can besubstituted for every hydrogen on the polymeric chain to form theconductive polymer, as represented by Formula V above. Further reactionresults in all amine-like nitrogens forming quaternary ammonium groups,as illustrated by Formula VI above. If the reaction is not carried tocompletion, only a portion of the hydrogen atoms on the polymer will besubstituted by cation or R groups, as illustrated by Formula IV above.

Where the "R⁺ " donor is an "R₃ OX" donor, an ether, R₂ O, e.g.,dimethyl ether, is given off in the reaction.

The above reactions of an R⁺ donor compound with a base type polymer,particularly polyaniline, for producing base-type conductive polymersare disclosed in the above co-pending applications, Serial Nos. 920,474and 013,305, and such disclosures are incorporated herein by reference.

Following treatment of the exposed portion 16 of the substrate with thespray 18 of chemical treating agent, the mask 12 is removed, leaving aconductive and resistive polyaniline region 20 surrounded by thepolyaniline non-conductive or insulating region 22, thus forming aresistor element 24.

Now referring to FIG. 2 of the drawings, a non-conductive sheet 26formed of a base-type polymer, such as polyaniline free-base, hasattached to the surfaces on opposite sides 28 thereof a metal, e.g.,steel, mask in the form of a peripheral frame 30 around all four sidesof the sheet, leaving an exposed central surface portion 32 ofnon-conductive polymer on each side of the sheet.

A spray of a treating agent 27 in the form of an R⁺ donor compound, suchas RX, as described above, is applied to opposite sides 28 of thenon-conductive polymer sheet 26 and contacting the exposed portions 32on opposite sides of the sheet. As a result of the reaction of thetreating agent with the exposed portions 32 of the polymer sheet 26,there are formed central conductive regions 34 of conductive polymer orconductive polyaniline on opposite sides 28 of the non-conductivepolymer sheet, with a non-conductive or insulating border portion 36around the conductive central portions 34, and a non-conductive orinsulating interior portion 38 (see FIG. 3) between the two conductiveregions 34. The resulting non-conductive polymer substrate containingthe separated conductive regions 34 can function as a capacitor.

If desired, the treating agent can be painted unto the exposed regions32 on both sides of the non-conductive polymer sheet 26. Further, ifdesired, the mask 30 can be omitted, and the entire area on both sidesof the non-conductive polymeric sheet 26 can be treated, as by sprayingor painting, with the treating agent to form conductive regions over theentire area on opposite surfaces of the polymeric sheet, separated bythe interior non-conductive region 38. The thickness of the conductiveregions 34 depends on the particular treating or doping agent employedand the period of time of exposure of the surfaces of the polymer sheetto the treating agent. Thus, the capacitance of the resulting capacitorcan be controlled by varying the thickness of the conducting regions 34.

In the processes illustrated in FIGS. 1 to 3, the non-conductive polymersubstrate is treated in preselected surface portions with a doping agentmolecule that covalently attaches to the polymer base site to formconductive regions surrounded or separated by dielectric or insulatingregions.

Conductive regions formed on a dielectric or insulating substrate, suchas polyaniline free-base, can be made to have conductivity gradients byreacting different parts of the substrate with a covalent doping agentfor different lengths of time, or by selective diffusion into a bulkbody of the base insulating polymer.

Thus, referring to FIG. 4, a block of base-type non-conductive polymer,such as polyaniline, at 40 can be immersed in a bath of covalent dopingagent or R⁺ donor compound 42, to a predetermined depth, as shown inFIG. 4(a), and by pulling the block of polymer 40 gradually from thetreating bath or solution until it is completely withdrawn, as indicatedin FIG. 4(b), the resulting polymer block 40, shown in FIG. 4(c), willhave a gradient of conductivity ranging from high conductivity at 44adjacent the bottom of the block to low conductivity at 46 adjacent theupper end of the polymer block. This is due to the fact that the region46 near the top of the polymer block has been withdrawn first andexposed to the treating agent 42 for the shortest time period, whereasthe region 44 adjacent the bottom of the block 40 has been exposed tothe treating bath for the longest time period and subjected to thegreater amount of diffusion of the liquid treating agent into the blockpolymer. Thus, a non-conductive polymer, such as polyaniline, can berendered conductive over a broad range of conductivity, for example,along its length, by selective diffusion, whereas such varyingconductivity cannot be imparted to a metal or to a conventional plasticmaterial.

Another electronic device which can be produced according to theinvention by covalent doping of certain portions of a non-conductivebase-type polymer, such as polyaniline, is an inductor or inductioncoil. This can be accomplished by a lathe-type process. Thus, as seen inFIG. 5, to a rod of base polymer 48 there is applied, from a suitablespray gun 50 a spray of cationic doping agent or R⁺ donor compound ofthe above types. The rod of base polymer 48 is rotated as in a clockwisedirection, viewing FIG. 5, and the spray gun 50 is moved or translatedin a horizontal direction at a constant rate, parallel to the axis ofthe rod, as indicated by the arrow 54. This results in the formation ofa helical line or coil of conductive polymer, indicated by dotted lines56, around the outer periphery of the non-conductive rod 48, defined bythe line of impingement of the spray 52 on the outer surface of the rod48.

Instead of employing a lathe-type process for fabricating an inductoraccording to the invention, as seen in FIG. 6, an inductor 58 can alsobe produced by utilizing a sheet or block 60 of non-conductive base-typepolymer, such as polyaniline, and, for example, by means of a paintbrush having a liquid covalent doping agent thereon, according to theinvention, painting a conductive loop 62 or any other desired shape, ona configuration of such loop or shape formed on the insulating sheet 60,by reaction of the covalent doping agent applied by the paint brush,with the non-conductive base-type polymer.

Also, employing one of the procedures noted above, e.g., the maskingprocedure illustrated in FIG. 1(b), or by the painting procedureillustrated in FIG. 6, a printed circuit board can be made by applying acovalent doping agent as described above to predetermined portions of abase-type non-conductive polymeric substrate, such as polyaniline, toprovide an entirely plastic printed circuit board which does not employa metal, such as copper, as the conductor.

The following are examples of practice of the invention:

EXAMPLE I

To a surface of a sheet of polyaniline free-bae was applied a stainlesssteel mask, as illustrated in FIG. 1(b). A 1 molar solution oftriethyloxonium hexachloroantimonate in methylene chloride was appliedby spraying over the exposed area 16 of the polyaniline substrate. Themask was removed, providing a conductive trace or region 20 on theinsulating polymer, to form a resistor. The conductive trace 20 remainsnon-diffusing over an extended time period, and the conductivity thereofis not degraded by exposure to water.

EXAMPLE II

A polyaniline free-base block polymer was exposed by spraying onopposite sides thereof, generally according to the procedure illustratedin FIG. 2, with pure dimethylsulfate. The resulting polymer substratehad conductive areas on opposite sides thereof, as illustrated at 38 inFIG. 3, and functions as a capacitor.

EXAMPLE III

A polyaniline free-base block polymer was immersed in a solution of 1molar methyl iodide in THF and the block was gradually completelywithdrawn from the treating solution, as illustrated in FIG. 4. Theresulting block polymer had a conductivity gradient ranging from highconductivity at the lower end of the block to low conductivity adjacentthe upper end of the block, as illustrated in FIG. 4(c).

EXAMPLE IV

An inductor was made according to the procedure illustrated in FIG. 5,by impinging a spray of trimethyloxonium hexafluorophosphate inmethylene chloride on a rotating cylindrical rod of polyanilinefree-base, while the spray was moved transversely of the rod andparallel to the axis thereof. A helical conductor was formed around theouter periphery of the rod.

From the foregoing, it is seen that the invention provides novelprocedure for fabricating novel electronic devices without employingmetal and resulting in light-weight, reliable devices formed entirely ofpolymeric material, and having stable conductivity and free ofconductivity degradation on contact with water.

While particular embodiments of the invention have been described forpurposes of illustration, it will be understood that various changes andmodifications within the spirit of the invention can be made, and theinvention is not to be taken as limited except by the scope of theappended claims.

What is claimed is:
 1. A process for producing an electronic device on anon-conductive polymer substrate which comprises applying a covalentdoping agent to a preselected portion of a base-type non-conductivepolymer substrate containing carbon-nitrogen linkages, said agent beingcapable of covalently binding to the nitrogens of said polymer, saidcovalent doping agent being an R⁺ donor compound containing an organiccation group, the R⁺ donor compound being selected from the groupconsisting of RX, R₃ OX, R₂ SO₄, R'SO₂ Cl, and R"₃ SiCl, where R, R' andR" are each selected from the group consisting of alkyl and aryl, and Xis selected from the group consisting of halogen, PF₆ ⁻, SbCl₆ ⁻ andbenzene sulfonate, and wherein the base-type non-conductive polymersubstrate is selected from the group consisting of polyaniline, itsnaphthyl and biphenyl derivatives, and alkyl and aryl substitutedpolyaniline and its alkyl and aryl substituted naphthyl and biphenylderivatives, and converting said preselected portion of said polymersubstrate to an electrically conductive polymer portion in which suchcation groups are covalently linked to the nitrogen atoms of saidpreselected polymer portion.
 2. The process of claim 1, said R⁺ donorcompound being dissolved in a solvent which does not react irreversiblywith said R⁺ donor compound.
 3. The process of claim 1, said R⁺ donorcompound being dissolved in a solvent selected from the group consistingof methylene chloride, tetrahydrofuran, acetonitrile, pyridine,dimethylsulfoxide and dimethylformamide.
 4. The process of claim 1, saidcovalent doping agent being applied to said preselected portion of saidpolymer substrate by spraying, immersion or brushing.
 5. The process ofclaim 1, including applying a suitable mask to said polymer substrateand exposing said preselected portion of said polymer substrate to saidcovalent doping agent.
 6. A process for producing an electronic deviceon a polyaniline substrate, which comprises applying to a preselectedregion of a base-type non-conductive polymer having the general formula:##STR4## where A is a carbon-containing aryl group and y is an integerranging from about 1 to about 1,000, a compound selected from the groupconsisting of RX, R₃ OX, R₂ SO₄, R'SO₂ Cl, and R₃ "SiQ, where Q is ahalogen, R, R' and R" are each selected from the group consisting ofalkyl and aryl, and X is selected from the group consisting of halogen,PF₆ ⁻, SbCl₆ ⁻, SO₂ Cl⁻ and benzene sulfonate, and forming anelectrically conductive polymer region on said non-conductive polymersubstrate.
 7. A process for producing an electronic device on anon-conductive polymer substrate which comprises applying a covalentdoping agent to a preselected portion of a non-conductive polyanilinesubstrate, said agent being capable of covalently binding to thenitrogens of said polyaniline, and converting said preselected portionof said polyaniline substrate to an electrically conductive polyanilineportion.
 8. A process for producing an electronic device on anon-conductive polymer substrate which comprises applying a covalentdoping agent to a preselected portion of a base-type non-conductivepolymer substrate containing carbon-nitrogen linkages, said agent beingcapable of covalently binding to the nitrogens of said polymer, andconverting said preselected portion of said polymer substrate to anelectrically conductive polymer portion, wherein the base-typenon-conductive polymer substrate is selected from the group consistingof polyaniline, its naphthyl and biphenyl derivatives, and alkyl andaryl substituted polyaniline and its alkyl and aryl substituted naphthyland biphenyl derivatives.
 9. A process for producing an electronicdevice on a polyaniline substrate, which comprises applyinq to apreselected region of a non-conductive polyaniline free-base substrate acompound selected from the group consisting of RX, R₃ OX, R₂ SO₄, R'SO₂Cl, and R₃ "SiQ, where Q is a halogen, R, R' and R" are each selectedfrom the group consisting of alkyl and aryl, and X is selected from thegroup consisting of halogen, PF₆ ⁻, SbCl₆ ⁻, SO₂ Cl⁻ and benzenesulfonate, and forming an electrically conductive polyaniline region onsaid non-conductive polyaniline substrate.
 10. The process of claim 9,said compound being in liquid form and applied to said preselectedregion by spraying or brushing, or by immersion of said substrate insaid liquid compound for a predetermined time.
 11. The process of claim9, including applying a suitable mask to said polymer substrate andexposing said preselected region of said polymer substrate to saidcompound.
 12. The process of claim 9 for producing a resistor, whereinsaid conductive polyaniline region is in the form of a resistive stripsurrounded by non-conductive polyaniline.
 13. The process of claim 9 forproducing a capacitor, wherein said non-conductive polyaniline free-basesubstrate is in the form of a block having substantially parallelopposite sides and applying said compound to preselected regions on saidopposite sides of said polyaniline substrate, and forming a conductivepolyaniline region on said opposite sides separated by a thickness ofnon-conductive polyaniline.
 14. The process of claim 9 for producing adevice having a conductivity gradient, wherein said compound is appliedto said preselected region of said substrate by immersing saidpolyaniline substrate in a liquid bath of said compound, and graduallywithdrawing said substrate from said bath, thereby exposing saidpreselected region of said substrate to said bath for different times,and forming a region of varying conductivity on said substrate.
 15. Theprocess of claim 9 for producing inductor, wherein said polyanilinesubstrate is in the form of a cylinder, and said compound in liquid formis applied as a spray on said cylinder substrate while rotating same andmoving said spray along a line parallel to the axis of said cylinder,and forming a helical coil of conductive polyaniline on saidnon-conductive polyaniline cylindrical substrate.
 16. The process ofclaim 9 for producing an inductor, wherein said polyaniline substrate isin the form of a sheet, and said compound in liquid form is applied tosaid preselected region in the form of a loop, and forming a conductivepolyaniline loop on said non-conductive polyaniline sheet.
 17. Theprocess of claim 9, wherein Q is chlorine.
 18. The process of claim 9,wherein said compound is RX, where R is alkyl and X is halogen.